Norris Andrew W, Hirshman Michael F, Yao Jianrong, Jessen Niels, Musi Nicolas, Chen Lihong, Sivitz William I, Goodyear Laurie J, Kahn C Ronald
Department of Pediatrics, University of Iowa, Iowa City, Iowa 52242, USA.
Endocrinology. 2008 Nov;149(11):5374-83. doi: 10.1210/en.2008-0100. Epub 2008 Jul 24.
In the setting of insulin resistance, agonists of peroxisome proliferator-activated receptor (PPAR)-gamma restore insulin action in muscle and promote lipid redistribution. Mice with muscle-specific knockout of PPARgamma (MuPPARgammaKO) develop excess adiposity, despite reduced food intake and normal glucose disposal in muscle. To understand the relation between muscle PPARgamma and lipid accumulation, we studied the fuel energetics of MuPPARgammaKO mice. Compared with controls, MuPPARgammaKO mice exhibited significantly increased ambulatory activity, muscle mitochondrial uncoupling, and respiratory quotient. Fitting with this latter finding, MuPPARgammaKO animals compared with control siblings exhibited a 25% reduction in the uptake of the fatty acid tracer 2-bromo-palmitate (P < 0.05) and a 13% increase in serum nonesterified fatty acids (P = 0.05). These abnormalities were associated with no change in AMP kinase (AMPK) phosphorylation, AMPK activity, or phosphorylation of acetyl-CoA carboxylase in muscle and occurred despite increased expression of fatty acid transport protein 1. Palmitate oxidation was not significantly altered in MuPPARgammaKO mice despite the increased expression of several genes promoting lipid oxidation. These data demonstrate that PPARgamma, even in the absence of exogenous activators, is required for normal rates of fatty acid uptake in oxidative skeletal muscle via mechanisms independent of AMPK and fatty acid transport protein 1. Thus, when PPARgamma activity in muscle is absent or reduced, there will be decreased fatty acid disposal leading to diminished energy utilization and ultimately adiposity.
在胰岛素抵抗的情况下,过氧化物酶体增殖物激活受体(PPAR)-γ激动剂可恢复肌肉中的胰岛素作用并促进脂质重新分布。肌肉特异性敲除PPARγ(MuPPARγKO)的小鼠尽管食物摄入量减少且肌肉中的葡萄糖处理正常,但仍出现肥胖。为了了解肌肉PPARγ与脂质积累之间的关系,我们研究了MuPPARγKO小鼠的能量代谢。与对照组相比,MuPPARγKO小鼠的活动量、肌肉线粒体解偶联和呼吸商显著增加。与这一发现相符的是,与对照同窝小鼠相比,MuPPARγKO动物的脂肪酸示踪剂2-溴棕榈酸的摄取减少了25%(P<0.05),血清非酯化脂肪酸增加了13%(P = 0.05)。这些异常与肌肉中AMP激酶(AMPK)的磷酸化、AMPK活性或乙酰辅酶A羧化酶的磷酸化没有变化有关,尽管脂肪酸转运蛋白1的表达增加,但仍会出现这些异常。尽管促进脂质氧化的几个基因的表达增加,但MuPPARγKO小鼠的棕榈酸氧化没有显著改变。这些数据表明,即使在没有外源性激活剂的情况下,PPARγ对于氧化型骨骼肌中通过独立于AMPK和脂肪酸转运蛋白1的机制进行正常脂肪酸摄取率也是必需的。因此,当肌肉中的PPARγ活性缺乏或降低时,脂肪酸处理会减少,导致能量利用减少并最终导致肥胖。